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Clinical Trials/CTRI/2025/08/093839
CTRI/2025/08/093839Not yet recruitingNot Applicable

A randomized comparative study to evaluate the analgesic effect of intravenous versus perineural dexmedetomidine as an adjuvant to bupivacaine in ultrasound-guided adductor canal block in patients undergoing total knee arthroplasty.

Sawai Maan Singh medical college1 site in 1 country70 target enrollmentStarted: September 1, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
70
Locations
1
Primary Endpoint
no significant difference in onset of sensory block between IV and perineural administration of dexmedetomidine as an adjuvant to bupivacaine in USG guided adductor canal block in patients undergoing total knee arthroplasty.

Study Overview

Brief Summary

The purpose of study is to compare which route between IV and perineural administration of Dexmedetomidine as an adjuvant to bupivacaine in USG guided adductor canal block is better for the onset of sensory block and analgesic effect.

We are doing this study because Total Knee Arthroplasty is associated with severe post operative pain and Adductor Canal Block is primarily a sensory block. Dexmedetomidine is a highly selective alpha-2 adrenergic agonist that is effectively used as a safe analgesic adjuvant. By finding which route (IV vs Perineural ) is better we can use dexmedetomidine as an adjuvant by that route safely.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 90.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Undergoing total knee replacement Informed written conscent American society of anesthesiologists grade 1,2 and 3.

Exclusion Criteria

  • Psychiatric illness Peripheral sensorineural deficit Allergic to study drugs Infection at site of block Compartment syndrome.

Outcomes

Primary Outcomes

no significant difference in onset of sensory block between IV and perineural administration of dexmedetomidine as an adjuvant to bupivacaine in USG guided adductor canal block in patients undergoing total knee arthroplasty.

Time Frame: 5min ,10mins,15 mins,20 mins postoperative

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Sawai Maan Singh medical college
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Harsimrat Kaur

Sawai Maan Singh Medical college

Study Sites (1)

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